Electronic and Ionic Conductivities Enhancement of Zinc Anode for Flexible Printed Zinc-Air Battery

Zinc-air battery is considered a promising candidate for future energy applications due to its high energy density, safety and low cost. However, poor battery performance and low efficiency of zinc utilization, resulted from passivation effect of the zinc anode, is a major challenge. Thus, in this work, investigation of electronic and ionic conductivities enhancement of the zinc anode for flexible printed zinc-air battery has been carried out. The anode was made from a zinc-based ink, prepared from a mixture of zinc and zinc oxide particles. Carbon black, sodium silicate (Na2SiO3) and bismuth oxide (Bi2O3) were investigated for implementation on the anode. The results showed that performance of the battery increased when carbon black was introduced into the anode as the presence of carbon black improved electronic conductivity of the anode. Again, the battery performed better when Bi2O3 orNa2SiO3 was introduced due to the formation of solid electrolyte interface (SEI) on the anode. The SEI inhibits passivation of zinc active surfaces and provides effective electrolyte access. The battery with Bi2O3 provided the best performance. The highest performance was observed when Bi2O3 content reached 26wt.%. No significant improvement was observed whenBi2O3 concentration increased higher than 26 wt.%.Zinc-air battery is considered a promising candidate for future energy applications due to its high energy density, safety and low cost. However, poor battery performance and low efficiency of zinc utilization, resulted from passivation effect of the zinc anode, is a major challenge. Thus, in this work, investigation of electronic and ionic conductivities enhancement of the zinc anode for flexible printed zinc-air battery has been carried out. The anode was made from a zinc-based ink, prepared from a mixture of zinc and zinc oxide particles. Carbon black, sodium silicate (Na2SiO3) and bismuth oxide (Bi2O3) were investigated for implementation on the anode. The results showed that performance of the battery increased when carbon black was introduced into the anode as the presence of carbon black improved electronic conductivity of the anode. Again, the battery performed better when Bi2O3 or Na2SiO3 was introduced due to the formation of solid electrolyte interface (SEI) on the anode. The SEI inhibits passivation of zinc active surfaces and provides effective electrolyte access. The battery with Bi2O3 provided the best performance. The highest performance was observed when Bi2O3 content reached 26 wt.%. No significant improvement was observed when Bi2O3 concentration increased higher than 26 wt.%

Near-infrared photoluminescence from molecular crystals containing tellurium

We report the observation of near-infrared photoluminescence from Te4(Ga2Cl7)2 and Te4(Al2Cl7)2 molecular crystals containing Te42+ polycations. The experimental and theoretical results clearly revealed that Te42+ polycation is one smart near-infrared emitter with characteristic emission peaks at 1252 and 1258 nm for Te4(Ga2Cl7)2 and Te4(Al2Cl7)2 crystals, respectively, resulting from the intrinsic electronic transitions of Te42+. Furthermore, it was also found that the emissions strongly depend on the excitation wavelengths for both Te4(Ga2Cl7)2 and Te4(Al2Cl7)2 samples, most possibly owing to the co-existence of other Te-related optically active centers. This research not only enriches the species of luminescent charged p-block element polyhedra and deepens the understanding of Te-related photophysical behaviors, but also may stimulate efforts for designing novel material systems using such active centers. It is also greatly expected that these sub-nanometer optically active species could exist in other systems such as glasses, polymers, and bulk optical crystals, and the stabilization of these centers in widely used hosts will pave the way for their practical applications

Photoluminescence from Bi5(GaCl4)3 molecular crystal

Bi5(GaCl4)3 sample has been synthesized through the oxidation of Bi metal by gallium chloride (GaCl3) salt. Powder X-ray diffraction as well as micro-Raman scattering results revealed that, in addition to crystalline Bi5(GaCl4)3 in the product, amorphous phase containing [GaCl4]- and [Ga2Cl7]- units also exist. The thorough comparison of steady-state and time-resolved photoluminescent behaviors between Bi5(GaCl4)3 product and Bi5(AlCl4)3 crystal leads us to conclude that Bi53+ is the dominant emitter in the product, which gives rise to the ultrabroad emission ranging from 1 to 2.7 micrometer. Detailed quantum chemistry calculation helps us assign the observed excitations to some electronic transitions of Bi53+ polycation, especially at shorter wavelengths. It is believed that our work shown here not only is helpful to solve the confusions on the luminescent origin of bismuth in other material systems, but also serves to develop novel broadband tunable laser materials

Microwave-assisted polyol synthesis of copper nanocrystals without using additional protective agents

We report the synthesis of 2 nm copper nanocrystals (Cu NCs)via a microwave-assisted polyol method without using additional protective and reducing agents. The Cu NCs are oxidation resistant and exhibit photoluminescence and highly stableproperties in a colloidal dispersion

Ultra-broad near-infrared photoluminescence from crystalline (K-crypt)2Bi2 containing [Bi2]2- dimers

For the first time, we report that a single crystal of (K-crypt)2Bi2 containing [Bi2]2+ displays ultra-broad near-infrared photoluminescence (PL) peaking at around 1190 nm and having a full width at the half maximum of 212 nm, stemming from the inherent electronic transitions of [Bi2]2+.The results not only add to the number of charged Bi species with luminescence, but also deepen the understanding of Bi-related near-infrared emission behavior and lead to the reconsideration of the fundamentally important issue of Bi-related PL mechanisms in some material systems such as bulk glasses, fibers, and conventional optical crystals

A Novel Physical Approach for Cationic-Thiolate Protected Fluorescent Gold Nanoparticles

Knowledge on the synthesis of cationically charged fluorescent gold nanoparticles (Au NPs) is limited because the electrostatic repulsion between cationic ligands on the surface of NP hinders the formation of small Au NPs (usually less than ca. 2 nm) during nucleation in solvents. We herein propose a novel methodology for a synthesis of water-dispersible, cationic-thiolate protected fluorescent Au NPs by the sputtering of Au into liquid matrix containing thiolate ligands. By controlling mercaptan concentration the size and photophysical characteristics of Au NPs were directly controlled, resulting in near IR fluorescence with a 0.9% of absolute quantum yield. Cationically charged fluorescent metal NPs are promising, especially in biological fields, and this work provides a novel methodology towards the synthesis of a new series of functional metal NPs

One-pot preparation of cationic charged Pt nanoparticles by the autocatalytic hydrolysis of acetylthiocholine

We propose a novel synthetic approach for cationic charged platinum nanoparticles via the autocatalytic hydrolysis of acetylthiocholine. This method can be extended to the platinum group of metals